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Osteoporosis due to cancer treatment: pathogenesis and management.

机译:癌症治疗引起的骨质疏松症:发病机理和治疗。

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摘要

Many therapeutic regimens in cancer treatment carry the risk of causing or favoring the development of osteoporosis. Therapies in which hypogonadism may occur are most relevant in this respect. Prompt hormone replacement therapy is indicated in these patients. In patients in whom this is undesirable because of a hormone-dependent tumor, the risk of osteoporosis should be assessed by means of osteodensitometry, and prophylactic or therapeutic measures should be instituted if necessary. Early intervention improves outcome because osteoporosis therapy is most effective in preventing deterioration of bone mass. There remains much uncertainty in assessing the risk of combination chemotherapy with regard to the development of osteoporosis. Negative effects on the skeleton have, however, been demonstrated for individual drugs, such as methotrexate and ifosfamide. Negative effects of the tumor itself on bone metabolism may aggravate the degree of osteoporosis. Detailed data and long-term experience to assess the risk are urgently needed in this area and constitute an important research topic for the coming years and decades. This review discusses the most prevalent mechanisms of osteoporosis caused by cancer treatment and outlines therapeutic strategies for the prevention and treatment of therapy-induced bone loss.
机译:癌症治疗中的许多治疗方案都有引起或促进骨质疏松症发展的风险。在这方面,可能发生性腺功能减退的疗法最相关。这些患者应立即进行激素替代治疗。对于因激素依赖性肿瘤而导致不良反应的患者,应通过骨密度测定法评估骨质疏松的风险,并在必要时采取预防或治疗措施。早期干预可以改善结局,因为骨质疏松症治疗最有效的预防骨量下降。关于骨质疏松症的发展,评估联合化疗的风险仍然存在很多不确定性。但是,对于单独的药物,例如甲氨蝶呤和异环磷酰胺,已证明对骨骼有负面影响。肿瘤本身对骨骼代谢的负面影响可能会加剧骨质疏松的程度。在这一领域,迫切需要详细的数据和评估风险的长期经验,并构成未来几年和几十年的重要研究课题。这篇综述讨论了由癌症治疗引起的骨质疏松症的最普遍机制,并概述了预防和治疗由治疗引起的骨质流失的治疗策略。

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